A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220244



Internal ID22364999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96157801..96157909hg38UCSC Ensembl
chr9:98920083..98920191hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14349630
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220244
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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